drugset / Trial / NCT00928668

Efficacy (Bronchoprotection) and Safety of Orally Inhaled BI 1744 CL in Patients With Intermittent Asthma

NCT00928668 ↗

Phase 2 Completed 32 enrolled Boehringer Ingelheim
RandomizedCrossoverDouble-blindTreatment

Summary

The primary objective of this study is to assess the efficacy (bronchoprotection) and safety of single doses of BI 1744 CL inhalation solution (2, 5, 10 and 20 mcg) delivered via the Respimat® inhaler, in patients with intermittent asthma.

Timeline

Start
2006-01
Primary completion
2006-10
Completion
—

Outcome

Met primary endpoint

registry Placebo vs Olodaterol (Olo) 2 mcg qd; p <0.0001; Mean Difference (Final Values) 1.157 (95% CI 0.657 to 1.657); Mixed Models Analysis NCT00928668 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Olodaterol Small molecule 2 ug Inhaled
Subject Olodaterol Small molecule 5 ug Inhaled
Subject Olodaterol Small molecule 10 ug Inhaled
Subject Olodaterol Small molecule 20 ug Inhaled

Indications